Mayo Clinic in Rochester
Rochester, Minnesota, 55905, United States
Location status: Recruiting
Location contact
Asma Chattha, MBBS
CONTACT
Candace F. Granberg, MD
PRINCIPAL_INVESTIGATOR
Chloe Schluttner
CONTACT
NCT Number: NCT02872532
This protocol is being designed to offer testicular tissue cryopreservation to male pediatric patients (0-17 years of age) with fertility threatening medical diagnoses or facing surgery, chemotherapy or radiation therapy that may cause loss of reproductive potential.
Interested in participating?
Request Info0 year–17 year
Male
Interventional
Not applicable
Rochester, Minnesota, 55905, United States
Location status: Recruiting
Asma Chattha, MBBS
CONTACT
Candace F. Granberg, MD
PRINCIPAL_INVESTIGATOR
Chloe Schluttner
CONTACT
Testicular tissue cryopreservation is currently considered experimental but offers the only opportunity for fertility preservation in pre-pubescent boys faced with a fertility threatening diagnosis or treatment plan.
After completion of study intervention, patients are followed up at 1-week post-surgery and then yearly thereafter.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
(All inclusion criteria must be met.)
Exclusion criteria
(Any exclusion criteria will disqualify.)
Testicular tissue will be removed
Time frame: 10-20 years
Contact information is provided by the study sponsor or research team.
Asma Chattha, MBBS
CONTACT
Chloe Schluttner
CONTACT
Mayo Clinic
Other
Testicular Tissue Cryopreservation for Fertility Preservation in Males Facing Fertility Threatening Diagnoses or Treatment Regimens
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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